The MAYFLOWERS study will: • Collect information about your baseline health in the 2 years before pregnancy using information from your medical records. • Collect information about you, and about your mental and physical health during and after pregnancy including lung function and weight. • Collect information about your pregnancy by reviewing your pregnancy and delivery records. • Collect information about your baby’s health by reviewing your baby’s pediatric records. • Collect information about your baby’s development by asking you specific questions. • Collect blood samples. A portion of the blood collected will be used to determine how much CFTR modulator is present (in those women who are taking them during pregnancy), and a portion will be stored for future research. This is called specimen banking. The MAYFLOWERS study also has an optional part called the Continuous Glucose Monitoring (CGM) sub-study. You can still participate in the MAYFLOWERS core study if you choose not to participate in this optional sub-study. The purpose of the CGM sub-study is to learn more about glucose (blood sugar) levels in pregnant women with CF. CGM tracks and records glucose levels throughout the day and night. A small CGM device will be attached to the back of your arm. It uses a tiny sensor inserted under the skin to check glucose levels while you are wearing it. The information will be used for the MAYFLOWERS study.